Traction forces produced by moving fibroblasts have been observed as d
istortions in flexible substrata including wrinkling of thin, silicone
rubber films. Traction forces generated by fibroblast lamellae were t
hought to represent the forces required to move the cell forwards. How
ever, traction forces could not be detected with faster moving cell ty
pes such as leukocytes and growth cones (Harris, A. K., D. Stopak, and
P. Wild. 1981. Nature (Lend.). 290:249-251). We have developed a new
assay in which traction forces produced by rapidly locomoting fish ker
atocytes can be detected by the two-dimensional displacements of small
beads embedded in the plane of an elastic substratum. Traction forces
were not detected at the rapidly extending front edge of the cell. In
stead the largest traction forces were exerted perpendicular to the le
ft and right cell margins. The maximum traction forces exerted by kera
tocytes were estimated to be similar to 2 X 10(-8) N. The pattern of t
raction forces can be related to the locomotion of a single keratocyte
in terms of lamellar contractility and area of close cell-substratum
contact.